A new optical chemical sensor is established for sensitive and selective spectrophotometric detection of copper based on the immobilization of 3‐(2‐methyl‐2,3‐dihydro‐1,3‐benzothiezol‐2‐yl)‐2H‐chromen‐2‐one on a triacetylcellulose membrane. Copper ions react with the immobilized ligand and cause an increase in the absorption of the membrane at 550 nm in universal buffer solution at pH = 6. The effects of pH, indicator concentration and reaction time on the immobilization of the ligand were studied. This optode exhibits a linear range of 7.0 × 10−7 to 1 × 10−4 mol l−1 of copper ion concentration with a limit of detection of 3.0 × 10−7 mol l−1. The response time of the newly designed optode is within 3 min. The effect of different possible interfering species was investigated and it was found that the sensor has very good selectivity. The proposed sensor benefits from advantages such as low cost, high stability, low detection limit, fast response time, reproducibility, relatively long lifetime, and good selectivity for Cu2+ ion determination among a large number of alkali, alkaline earth, transition and heavy metal ions. The sensor can readily be regenerated with thiourea solution and its response is reversible and reproducible (relative standard deviation < 1.4%). The proposed optode was applied successfully for the determination of Cu(II) in various samples.
Background:
Copper is one of several heavy metals. A low concentration of copper is vital for animals and plants, whereas it is highly toxic to aquatic plants and bacteria in a high concentration. Therefore, copper ions in water and food must be controlled, and as a result, the development of novel methods for the determination of copper in water samples is of interest.
Objective:
Different techniques have been proposed for copper ions extraction and determination. The magnetic solid -phase extraction method is considered superior to the other method for simplicity, its higher enrichment, and the need for lower quantities of solvents. The novel modified magnetite nanoparticles as the sorbent, along with the atomic absorption spectrometry analysis, can be a low‐cost, simple and rapid method for this propose.
Methods:
Traces of Cu(II) in environmental samples were preconcentrated using a novel magnetic adsorbent developed based on 2,2´-((1E,1´E)-hydrazine-1,2-diylidenebis(methanylylidene)) diphenol coated magnetite nanoparticles. The influence of ligand concentration, amount of adsorbent, pH, type of eluent, sample volume, and effects of interfering ions was optimized. The adsorbed species were eluted for analysis through atomic absorption spectrometry.
Results:
A linear calibration curve was recorded from 2 to 40 µg ml-1 (r2= 0.999) under optimal conditions, and the detection limit of the method was as low as 1.6 µg ml-1. Also, good recoveries were obtained for the real sample analysis.
Conclusion:
The developed procedure constituted a rapid extraction, a low-cost and efficient method, and was used for the analysis of copper ions in the tap, river, and lake water.
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